SML0055
Securinine
≥98% (HPLC)
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About This Item
Empirical Formula (Hill Notation):
C13H15NO2
CAS Number:
Molecular Weight:
217.26
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
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Quality Level
assay
≥98% (HPLC)
form
powder
optical activity
[α]/D -980 to -1015 (C=1, MeOH)
color
yellow
solubility
DMSO: ≥25 mg/mL
storage temp.
2-8°C
SMILES string
O=C1O[C@@]23C[C@@H](C=CC2=C1)N4CCCC[C@H]34
InChI
1S/C13H15NO2/c15-12-7-9-4-5-10-8-13(9,16-12)11-3-1-2-6-14(10)11/h4-5,7,10-11H,1-3,6,8H2/t10-,11-,13+/m1/s1
InChI key
SWZMSZQQJRKFBP-WZRBSPASSA-N
Application
Securinine was used as a standard in the synthesis of the members of Securinega alkaloid family.[1]
Biochem/physiol Actions
Securinine is a GABAA receptor antagonist which has been found to increase p73 protein expression
Securinine is an alkaloid widely in traditional folk medicine. Long known as a GABAA antagonist, securinine was recently found to up-regulate p53 protein and to modulate the related family member p73 protein in a p53-dependent fashion, inducing p73 in the HCT116 p53(-) cells and down-regulating it in the p53(+) cells. Induction of proapoptotic protein p73 only in p53 cells could be used to target cancer cells preferentially. Securinine has been found to induce p53-independent, p73-dependent apoptosis in RKO colon cancer cells.
Features and Benefits
This compound is featured on the GABAA Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Articles
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H Pu et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 24(4), 278-280 (2003-02-18)
Pharmacological activities of virosecurinine (Vse) and securinine (Sec) were studied. The results showed that acute toxicity of Vse was 1/13.6 that of Sec, and Vse had no convulsive effects on rats or frogs, while Sec had. The results also showed
Kirk Lubick et al.
Journal of leukocyte biology, 82(5), 1062-1069 (2007-08-19)
Innate immune cell stimulation represents a complementary approach to vaccines and antimicrobial drugs to counter infectious disease. We have used assays of macrophage activation and in vitro and in vivo phase II Coxiella burnetii infection models to compare and contrast
Jung-Hsuan Chen et al.
Organic letters, 14(17), 4531-4533 (2012-08-24)
Total syntheses of (±)-securinine and (±)-allosecurinine that employ a tandem rhodium carbenoid-initiated Claisen/α-ketol rearrangement sequence as a key step are described.
Global Trade Item Number
| SKU | GTIN |
|---|---|
| SML0055-25MG | 04061832925578 |
| SML0055-5MG | 04061837076671 |